A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585174



Internal ID6972698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9457372..9460218hg38UCSC Ensembl
Innerchr1:9457384..9460207hg38UCSC Ensembl
Outerchr1:9457361..9460230hg38UCSC Ensembl
chr1:9517431..9520277hg19UCSC Ensembl
Innerchr1:9517443..9520266hg19UCSC Ensembl
Outerchr1:9517420..9520289hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382847
hg192847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9850212
SamplesHG01847
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585174
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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